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Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

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Description scientific article published on 23 August 2018
Author/s

author: Svetlana Gorokhova  Denise Horn  Delphine Héron  Nuria C Bramswig  Lara Segebrecht  Valentina Stanley  Camille Trautman  Jennifer McEvoy-Venneri  Laurent Villard  Maha Zaki  Mahmoud Y Issa 

Publication date August 23, 2018
Language English
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